Department of Preventive Medicine and Public Health, School of Medicine, University of Valencia, Valencia, Spain.
Cardiovasc Diabetol. 2012 Nov 6;11:137. doi: 10.1186/1475-2840-11-137.
Although the fat mass and obesity (FTO) and melanocortin-4 receptor (MC4R) genes have been consistently associated with obesity risk, the association between the obesity-risk alleles with type 2 diabetes is still controversial. In some recent meta-analyses in which significant results have been reported, the associations disappeared after adjustment for body mass index (BMI). However gene-diet interactions with dietary patterns have not been investigated. Our main aim was to analyze whether these associations are modulated by the level of adherence to the Mediterranean Diet (MedDiet).
Case-control study in 7,052 high cardiovascular risk subjects (3,430 type 2 diabetes cases and 3,622 non-diabetic subjects) with no differences in BMI. Diet was assessed by validated questionnaires. FTO-rs9939609 and MC4R-rs17782313 were determined. An aggregate genetic score was calculated to test additive effects. Gene-diet interactions were analyzed.
Neither of the polymorphisms was associated with type 2 diabetes in the whole population. However, we found consistent gene-diet interactions with adherence to the MedDiet both for the FTO-rs9939609 (P-interaction=0.039), the MC4R-rs17782313 (P-interaction=0.009) and for their aggregate score (P-interaction=0.006). When adherence to the MedDiet was low, carriers of the variant alleles had higher type 2 diabetes risk (OR=1.21, 95%CI: 1.03-1.40; P=0.019 for FTO-rs9939609 and OR=1.17, 95%CI:1.01-1.36; P=0.035 for MC4R-rs17782313) than wild-type subjects. However, when adherence to the MedDiet was high, these associations disappeared (OR=0.97, 95%CI: 0.85-1.16; P=0.673 for FTO-rs9939609 and OR=0.89, 95%CI:0.78-1.02; P=0.097 for MC4R-rs17782313). These gene-diet interactions remained significant even after adjustment for BMI. As MedDiet is rich in folate, we also specifically examined folate intake and detected statistically significant interaction effects on fasting plasma glucose concentrations in non-diabetic subjects. However these findings should be interpreted with caution because folate intake may simply reflect a healthy dietary pattern.
These novel results suggest that the association of the FTO-rs9939609 and the MC4R-rs17782313 polymorphisms with type 2 diabetes depends on diet and that a high adherence to the MedDiet counteracts the genetic predisposition.
尽管脂肪量和肥胖(FTO)和黑皮质素 4 受体(MC4R)基因一直与肥胖风险相关,但肥胖风险等位基因与 2 型糖尿病之间的关联仍存在争议。在一些最近的荟萃分析中,报道了显著的结果,在调整体重指数(BMI)后,这些关联消失了。然而,基因-饮食与饮食模式的相互作用尚未得到研究。我们的主要目的是分析这些关联是否受到地中海饮食(MedDiet)依从性水平的调节。
在 7052 名高心血管风险受试者(3430 例 2 型糖尿病病例和 3622 例非糖尿病受试者)中进行病例对照研究,两组之间 BMI 无差异。饮食通过经过验证的问卷进行评估。确定 FTO-rs9939609 和 MC4R-rs17782313。计算累积遗传评分以测试加性效应。分析基因-饮食的相互作用。
在整个人群中,两种多态性均与 2 型糖尿病无关。然而,我们发现与 MedDiet 依从性存在一致的基因-饮食相互作用,这两种多态性都存在(FTO-rs9939609:P 交互=0.039,MC4R-rs17782313:P 交互=0.009),以及它们的累积评分(P 交互=0.006)。当 MedDiet 的依从性较低时,携带变异等位基因的个体患 2 型糖尿病的风险更高(OR=1.21,95%CI:1.03-1.40;P=0.019 用于 FTO-rs9939609 和 OR=1.17,95%CI:1.01-1.36;P=0.035 用于 MC4R-rs17782313)比野生型受试者。然而,当 MedDiet 的依从性较高时,这些关联就消失了(OR=0.97,95%CI:0.85-1.16;P=0.673 用于 FTO-rs9939609 和 OR=0.89,95%CI:0.78-1.02;P=0.097 用于 MC4R-rs17782313)。即使在调整 BMI 后,这些基因-饮食的相互作用仍然显著。由于 MedDiet 富含叶酸,我们还特别检查了叶酸摄入量,并在非糖尿病患者中检测到空腹血糖浓度的统计学显著的相互作用效应。然而,这些发现应谨慎解释,因为叶酸的摄入量可能仅仅反映了健康的饮食模式。
这些新的结果表明,FTO-rs9939609 和 MC4R-rs17782313 多态性与 2 型糖尿病之间的关联取决于饮食,并且对 MedDiet 的高度依从可以抵消遗传易感性。